• No criminal background checks on employees, including the abortionist. February 23 2015 Department of Health Inspection 
• The facility failed to report the emergency transfer of a patient who hemorrhaged after her abortion. No investigation or report to the Department and Patient Safety Authority were provided. April 1 2014 Department of Health Inspection
• Upon review of the facility’s patient safety committee meeting notes, there was no mention of the patient’s transfer to the emergency room by ambulance in the meetings. The committee made no review or recommendations regarding this patient’s adverse event. November 30 2017 Department of Health Inspection
• The facility failed to protect the confidentiality of patient’s personal health information. Medical records were not kept confidential. April 1 2014 Department of Health Inspection
• Expired medications were in use in the emergency kit. August 23 2017 Department of Health Inspection
• The facility failed to ensure a licensed nurse was in attendance in the recovery room during the time the patient was recovering following a surgical abortion. March 15 2018 Department of Health Inspection
• The facility failed to ensure only nonflammable agents were used for pre-surgical skin preparations. Inspection revealed Hibiclens was used by the abortionist to prep the cervix prior to the surgical abortion. March 15 2018 Department of Health Inspection
• The facility failed to ensure women presenting to the facility for an abortion were provided the Department of Health printed materials which describe the preborn child; the list of agencies which offer alternatives to abortion; the right to review the printed materials; and a copy provided to her free of charge if she chooses to review it. This is a violation of the woman’s right to know. March 15 2018 Department of Health Inspection
• The facility failed to ensure all required equipment was contained in the facility's cut-down instrument tray in each procedure room. April 25 2019 Department of Health Inspection 

The facility failed to ensure chemicals used to clean instruments were not stored with patient supplies and medications and the facility failed to ensure food was not stored in a facility identified dirty area.

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The facility failed to administer RhoGAM injections to patients who are Rh negative. If the blood from Rh-positive baby enters the mother’s Rh-negative bloodstream, there will be a blood type mismatch. This is called Rh-incompatibility. Her immune system sees the baby’s red blood cells as “foreign” and will produce antibodies that try to eliminate them. RhoGAM, IF given to her at the right time, will prevent her immune system from reacting to the baby’s blood. Failure could lead to infertility. The facility failed to administer this necessary medication to the patients.

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Failed to enforce policies for two person sign off on drug administration.

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